Difference between revisions of "User:Z3292017"
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Types of application uses: detection by Western blotting, Immunoprecipitation, Immunofluorescence | Types of application uses: detection by Western blotting, Immunoprecipitation, Immunofluorescence | ||
− | References using E-cadherin antibody: | + | References using E-cadherin antibody: <pubmed>PMID: 20609236</pubmed> |
Revision as of 11:09, 18 April 2013
Lab Attendance
Lab 1 - Z3292017 (talk) 15:07, 14 March 2013 (EST)
Lab 2 - Z3292017 (talk) 15:03, 21 March 2013 (EST)
Lab 3 - Z3292017 (talk) 15:11, 28 March 2013 (EST)
Lab 4 - Z3292017 (talk) 16:12, 11 April 2013 (EST)
Individual Assessments
Lab 1
Structural features comparison of the proteomes in the three superkingdoms
Reference
<pubmed>PMC3320622</pubmed>
Copyright
Copyright Pancsa and Tompa. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
--Mark Hill (talk) 10:32, 9 April 2013 (EST) Relevant article on comparison of prokayotes and eukaryotes.
Lab 2
<pubmed>PMC3585150</pubmed>
In this study the researchers used Super-Resolution Microscopy in order to attempt to understand the gag proteins and envelope recruitment and how exactly the HIV-1 virus is incorporated into the cell (which was previously not known). They were able to see the GAG assembly sites along with teh HIV-1 envelope proteins in the envelope expressing cells. It was discovered that the envelope accumulation outside of and surrounding the GAG assemblies (rather than directly being in contact with it) was able to assist the spread of the virus in vivo.
--Mark Hill (talk) 10:39, 9 April 2013 (EST) This is a reasonable summary of the article on Super-Resolution Microscopy. You may have considered explaining further why this technique was better than existing techniques, e.g. resolution, localisation. You have used as explained in class the Pubmed referencing format correctly.
Lab 3
Lab 4
Antibody against an adhesion junction protein - E-Cadherin
Data sheet: [E-Cadherin]
Type of antibody: Monoclonal
Species raised in: Mouse
Species reacts against: human breast carcinoma cell line T471
Types of application uses: detection by Western blotting, Immunoprecipitation, Immunofluorescence
References using E-cadherin antibody: <pubmed>PMID: 20609236</pubmed>